US2951939A - Devices for analyzing fluid mixtures by absorption of rays - Google Patents

Devices for analyzing fluid mixtures by absorption of rays Download PDF

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US2951939A
US2951939A US582875A US58287556A US2951939A US 2951939 A US2951939 A US 2951939A US 582875 A US582875 A US 582875A US 58287556 A US58287556 A US 58287556A US 2951939 A US2951939 A US 2951939A
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Luft Karl
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Office National dEtudes et de Recherches Aerospatiales ONERA
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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/31Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
    • G01N21/35Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
    • G01N21/37Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light using pneumatic detection

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  • the chief object of my invention is to permit, by means of a single beam, of obtaining an improved stability [influences during their travel, which makes it relaand alsoto increase selectively and to permit a relatively easy'compensation of disturbing effects
  • the device according tomy invention is characterized r intha-t the selective receiver substance is divided into two idistinct 'portions located in respective cells, said portions rzb'eing constitutedby the same fluid, through which passes:
  • the difference or the ratio thus measured supplies an indication of the importance of the partial absorption undergone by the ray beam during its passage through the sample cell, and therefore it permits of measuring the amount of the component that is considered in the mixture present in said cell.
  • Fig. 1 diagrammatically shows a first embodiment of my invention.
  • Fig. 2 is a similar view of a modification.
  • Figs. 3 and 4 show details of the device illustrated by Fig. 2.
  • the analyzer-device for gaseous mixtures illustrated by the drawings includes a source 1 supplying a beam of infra-red rays, this source being for instance constituted by a filament, such as a Nichrome filament heated at about 700 C., which thus emits a wide continuous band of rays.
  • a source 1 supplying a beam of infra-red rays, this source being for instance constituted by a filament, such as a Nichrome filament heated at about 700 C., which thus emits a wide continuous band of rays.
  • a rotating shutter 2 having for instance the shape of a semi-circular plate or of a disc provided with holes, this shutter being driven by a motor 3 and serving periodically to cut off the ray beam-with a given frequency.
  • This periodically interrupted beam is made to pass through a sample cell 4 containing the'mixture to be analyzedf
  • This ray beam when issuing from cell 4, then p'assesthrough two detector cells 5 and 6 disposed .one behind the other and filled with the samereceiver gas, which may be either the gas to be measured in the .mixture present in cell 4, or a mixture containing, in
  • the detector cells 5 and 6 may be .filledieither withpure CO or with a mixture of CO .(N )'or with argon (Ar).
  • both ends of cells 4 and 5 and the inlet end of cell 6 are made of a materiala through whichtheraysare able to pass without any material absorptionthereof.
  • i 1 v '7 T p ,In I order to measure the selective absorption ofthe jinfra-redrays into the two detector cells 5 and 6, I may 45 f use any suitable parameter such as the variation of temperature or the variation of pressure in these cells.
  • these chambers When use is made, as parameter, of the pressure, these chambers may be connected with a diaphragm condenser the electrodes of which are, constituted by a movable diaphragm 7 and a fixed armature8.
  • the variations of capacity produced by the displacements of diaphragm 7 are transformed into voltage variations, which are amplified in anamplifier 9 and measured in a suitable measurement instrument 10.
  • a diaphragm 11, interposed between the two detector cells 5 and 6, serves to obtain zero adjustment.
  • the absorption band of a gas is characterized by a plurality of lines the intensities of which are distributed, according to the Maxwell-Boltzmann law, and the widths It is known thatthe layer each line is of a thickness considerably smaller than that of the layer of gas necessary for wholly absorbing the rays the Wave-length of which corresponds to the marginalportions of the lines.
  • a layer o* f 'gas the thickness of which is insufl'icient for Wholly absorbing the rays the wavelengths of which correspond .tothe" absorption band of the gas that is considered,
  • detector cell the height of which is chosen so that it absorbs onlyga portion of the rays that enter it, has a preferential absorption efiect on the wave-lengths corresponding to the middle portions of the linesor the absorption bands, whereas detector cell 6 receives a ray beam from which have already been absorbed most of the rays corresponding to the marginal portions of the lines, whereby this cell 6 absorbs chiefly rays corresponding to the marginal portions of the lines.
  • the apparatus is adjusted in such manner that the amounts of energy absorbed inithe two respective detector cells 5 and 6 are substantially equal and produce an approximative equality of the measured parameters when the gaseous mixture in cell 4 does not include the gas to be measured, so that, in the ray beam emitted from source 1 with a given intensity, the wavelengths corresponding to the absorption band of the gas to be measured pass through said cell 4 without being weakened.
  • the absorption in cell 5 of the rays the wave-lengths of, which are those of the middle portions of the lines may be as high as 90%.
  • this mixture absorbs chiefly a portion of the rays the wave-lengths of which correspond to the middle portions of the lines.
  • the height of the second detector cell 6 is several times greater than that of the first cell 5.
  • the height of cell 4 must be determined in such manner that, even for the highest possible concentration of the gas to be measured in the mixture present in this cell, the maximum absorption of the rays the wave-length of which corresponds to the middle portions of the lines or" the absorption band of the gas to be measured does not exceed a predetermined percentage.
  • the value of this percentage may be for instance 20% and this for the more intensive lines which,
  • N nitrogen
  • cells 5 and 6 were filled with 'ratus. parent bottom and to dispose across the same beam other a mixture of CO and N in which the percentage of CO was 11%.
  • the height of cell 4- was 25 mm., that of cell 5, 10 mm. and that of cell 6, 25 mm.
  • the sensitiveness was practically constant.
  • the means according to the invention have the advantage of a high selectivity.
  • the absorbed energy due to the presence of a disturbing gas having an absorption band which overlaps that of the gas to be measured is generally more or less the same in the two detector cells and is therefore at least partly compensated for.
  • the measurement effect obtained with the device according to my invention is due to the preferential absorption bythe first detector cell of rays the wave-lengths of which correspond to the middle portions of the most intensive lines of the absorption band of the gas to be measured, whereas this preferential effect does not act for the parasitic absorption of the disturbing gas if the middle portions of the lines which overlap only by their edges are sufiiciently spaced apart.
  • the invention easily permits of taking supplementary compensatory steps, such for instance as filtering by gaseous layers constituted by disturbing gases and interposed across the path of travel of the beam, either before cell 5 or between cells 5 and 6.
  • the residual disturbing effect When the residual disturbing effect isinegative, it may be compensated by adding to the receiver gas some amount of the disturbing gas so as to produce a positive compensation efiect of the same magnitude.
  • the height of the cell 4 containing this mixture must be sufliciently great to give the sensitiveness necessary for measurement of concentrations which are normally very low.
  • concentration of the gas to be measured increases suddenly beyond the limit that has been expected and the measurement may then become ambiguous because the difierence of the absorptions in cells 5 and 6 starts decreasing when the rays are more and more absorbed in the cell which contains the mixture.
  • the ray beam which passes through cells 4, and 6 is not only periodically cut off at a given frequency, before entering cell 5, but also once more periodically cut off with a different frequency as it is passing between cells 5 and 6.
  • the first mentioned interruption of the ray beam is obtained, in Fig. 1, by a rotating shutter 2 located upstream of cell 4.
  • the second intermption of the beam is obtained by means of another shutter 13 disposed between cells 5 and 6.
  • the two shutters 12 and 13 may be fixed to the same shaft and driven by the same motor 3. However the frequencies of interruption must be different for the two elements 12 and 13.
  • the first shutter 12 gives a frequency of interruption of the beam leaving cell 4 equal to h, whereas the second shutter 13 gives-a frequency of interruption f; for a portion of the beam entering cell 6.
  • Fig. 3 shows a construction of shutter 12, the circle in dotted lines indicating the cross section s of the beam.
  • shutter 12 instead of being located between cells 4 and 5, might have been disposed between source 1 and cell 4.
  • the amounts of energy due to selective ray absorption in cells 5 and 6 act upon the opposed faces of the movable diaphragm 7 of the diaphragm condenser.
  • the first one designated by e is a differential signal of frequency f;
  • the second one designated by 2 and superimposed upon the first one, has a frequency 3.
  • the two signals e and e after being amplified in amplifier 9, are separated and rectified through a known device 14- 15 containing filtering means. Their ratio is measured by a potentiometric measurement instrument 16.
  • signal e of frequency f remains practically constant for normal variations of the concentration of the gas to be measured and starts decreasing only if this concentration is substantially in excess of the normal concentration value. If the absorption in cell 4 exceeds the limit that has been fixed, the reduction of the rays selectively absorbed in cells 5 and 6 has an analogous effect on the two signals e and e whereby the ratio measured by instrument 16 keeps increasing and does not risk to become ambiguous.
  • Another method for measuring the ratio of signals e and 2 would consist in producing a single frequency of interruption with the twoshutters 12 and 13 but in bringing these two interruptions in difference of phase, so
  • the two'signals e and e can be separated by phase discrimination by means of synchronized switches.
  • What ever be the. means used for measuring the ratio of the two signals e; and e Ieliminate not only any ambiguityintheresult off the measurement but I obtain at the same time that the 'resultof the measurement is still less influencedby the possible presence'in themixture of other'gases having absorption bands overlapping those of the gas to be, measured.
  • the absorption produced by such gases reduces boththe main signal and the auxiliary signal so that" the ratio remains practically unchanged.
  • the measurement becomes independent of the variations that may be undergone either by the intensity of the source of the ray beam or by the amplification.
  • the two detector cells are not necessarily both connected with a differential element such as a diaphragm condenser. They might remain separate from each other.
  • the invention does not exclude the case where the gases present in the detector cells have different pressures and concentrations so as to facilitate measurement.
  • a fluid analyzer apparatus for measuring the relative amount, in amixture of fluids, of a given fluid component capable of selectively absorbing rays of given wave bands from a given ray beam passing therethrough which comprises, in combination, a sample cell arranged to be filled with said fluid mixture to be analyzed, two detector cells both containing the same fluid, said last mentioned fluid having substantially the same ray absorption wave bands as said component, means for passing the same ray beam through said sample cell and both of said detector cells in series, and means connected to both said detector cells for comparing the respective amounts of energy absorbed by said two detector cells from said ray beam.
  • a fluid analyzer apparatus for measuring the relative amount, in a mixture of fluids, of a given fluid component capable of selectively absorbing rays of given wave bands from a given rays beam passing theremeans connected to both said detector cells for measuring the difference between the respective amounts of energy absorbed by said two detector cells from said ray beam.
  • An apparatus further including a shutter disposed between said two detector cells 7 and adjustable to indicate the concentration of the gas to'be measured when the same amounts of energy are absorbed from -said'two detector cells, respectively.
  • An apparatus further includ ing. 'means' for measitring the. absoluterv alue of the amount of energy. absorbed from said' ray beam by the lastjdeteetorcelhv. a I 1 a 16
  • An apparatl is according to claim 5 'in which the two last mentioned means are means for producing signals re'stiec't-ively proportional to the difference, of the amounts of energy absorbed from-said two detector .cell

Description

Sept. 6, 1960 I K. LUFT 2,951,939
DEVICES FOR ANALYZING FLUID MIXTURES BY ABSORPTION OF RAYS Filed ma 4, 1955 v m1 a 2g].
INVENTUR 6% ATTOHNEY% Un cdStatcs.P te tfQ FOR ANALYZING FLUID MIXTURES BY ABSORPTION RAYS Karl Loft, Massy, France, assignor to Oflice National dEtudes et de Recherches Aeronautiques 0.N.E.R.A.,
.Chatillon-sous-Bagneaux, France, a French society Filed May 4, 1956, Ser. No. 582,875 .I"Claims priority, application France. May 7, 1955 6 Claims, Cl. 250-435 I "DEVICES fiuid' to be measured itself, a fluid having substantially .the same absorption wave bands as said component to be measured.- Such a receiver layer detects only the rays located in the absorption bands of :the fluidor gas to be measured or-possibly of other gases insofar as the ab- ,sorption .bands of these. last mentioned gases overlap those of the gas to be measured. Therefore this receiver :isselective receiver. i i s Gas analyzers of this kind generally utilize two identical selective receiverswhich. absorb the rays of predetermined iwave-length contained in two ray beams one of which, before reaching itsfselective receiver, has: passed :through a sample cell containing the mixture to. be analyzed, whereas the other beam, before. reaching its respective receiver, has passed through acell containing .a gas having no absorptionieifect for the wave-lengths 111a are considered and serving only as comparison gas.
' 7 However the use of two different beams involves some ldifii clulties. Firstgthe'se beams'maybe subjected to differ.-
tivel'y diflicult to obtain a stable-zero iof the device. :Fiu'thermore, when the mixtures to be analyzed include components the absorptionbandsof which overlap each other,laccuracy of the, measurement is often insufficient, -sincef compensation of the disturbingr effects, by means of i'sirriple methods, is very difiicult. i
It has also ,been proposed to utilize alsingle beam instead of two beams and to measure the difference between "the.,seleetive absorption effect in a first receiver layer ji'c'onstituted by the gas to be measured and the eifect of hon-selective absorptionof the residual rays. However, by thus measuring the difierence between a selective effect a. total and non-selective effect other difiiculties are,
"experienced which resultfrom the entirely difierent nature f of'these two phenomena.
The chief object of my invention is to permit, by means of a single beam, of obtaining an improved stability [influences during their travel, which makes it relaand alsoto increase selectively and to permit a relatively easy'compensation of disturbing effects The device according tomy invention is characterized r intha-t the selective receiver substance is divided into two idistinct 'portions located in respective cells, said portions rzb'eing constitutedby the same fluid, through which passes:
the ray beam which has-already passed through the sample Ixc'ell .which contains the mixture to. be'ana'lyzed'rneasureif nient means being provided to measure either the dineri ence'. between, or the ratio of, the amounts of energy ab- .L so'rbed from said r'ay beam by said tWodetector cells, re-
. 2 V 1 spectively. The difference or the ratio thus measured supplies an indication of the importance of the partial absorption undergone by the ray beam during its passage through the sample cell, and therefore it permits of measuring the amount of the component that is considered in the mixture present in said cell.
Preferred embodiments of my invention will be hereinafter described wtih reference to the accompanying drawings, given merely by way of example and in which:
. Fig. 1 diagrammatically shows a first embodiment of my invention. v
Fig. 2 is a similar view of a modification.
Figs. 3 and 4 show details of the device illustrated by Fig. 2.
The analyzer-device for gaseous mixtures illustrated by the drawings includes a source 1 supplying a beam of infra-red rays, this source being for instance constituted by a filament, such as a Nichrome filament heated at about 700 C., which thus emits a wide continuous band of rays. I provide, downstream of this my source 1, a rotating shutter 2 having for instance the shape of a semi-circular plate or of a disc provided with holes, this shutter being driven by a motor 3 and serving periodically to cut off the ray beam-with a given frequency.
This periodically interrupted beam is made to pass through a sample cell 4 containing the'mixture to be analyzedf This ray beam, when issuing from cell 4, then p'assesthrough two detector cells 5 and 6 disposed .one behind the other and filled with the samereceiver gas, which may be either the gas to be measured in the .mixture present in cell 4, or a mixture containing, in
addition to said gas to be measured, another gas which is non absorbent. For instance, if the gas to be measured in the mixture contained in cell 4 iscarbon monoxide .(CO), the detector cells 5 and 6 may be .filledieither withpure CO or with a mixture of CO .(N )'or with argon (Ar).
with nitrogen In order to enable the ray beam to pass successively thr'ough'cells 4, 5 and 6, both ends of cells 4 and 5 and the inlet end of cell 6 are made of a materiala through whichtheraysare able to pass without any material absorptionthereof. i 1 v '7 T p ,In I, order to measure the selective absorption ofthe jinfra-redrays into the two detector cells 5 and 6, I may 45 f use any suitable parameter such as the variation of temperature or the variation of pressure in these cells.
When use is made, as parameter, of the pressure, these chambers may be connected with a diaphragm condenser the electrodes of which are, constituted by a movable diaphragm 7 and a fixed armature8. The variations of capacity produced by the displacements of diaphragm 7 are transformed into voltage variations, which are amplified in anamplifier 9 and measured in a suitable measurement instrument 10.
A diaphragm 11, interposed between the two detector cells 5 and 6, serves to obtain zero adjustment.
' The operation of my device is based upon phenomena a shortdescription of which will now be given.
The absorption band of a gas is characterized by a plurality of lines the intensities of which are distributed, according to the Maxwell-Boltzmann law, and the widths It is known thatthe layer each line is of a thickness considerably smaller than that of the layer of gas necessary for wholly absorbing the rays the Wave-length of which corresponds to the marginalportions of the lines. In other words, a layer o* f 'gas the thickness of which is insufl'icient for Wholly absorbing the rays the wavelengths of which correspond .tothe" absorption band of the gas that is considered,
has a moreintensive effect for the wave-lengths corresponding to the middle portion of said lines than for the wave-lengths corresponding to the marginal portions of said lines. it
If these considerations are applied to the present invention, it is found that detector cell the height of which is chosen so that it absorbs onlyga portion of the rays that enter it, has a preferential absorption efiect on the wave-lengths corresponding to the middle portions of the linesor the absorption bands, whereas detector cell 6 receives a ray beam from which have already been absorbed most of the rays corresponding to the marginal portions of the lines, whereby this cell 6 absorbs chiefly rays corresponding to the marginal portions of the lines.
Preferably, the apparatus is adjusted in such manner that the amounts of energy absorbed inithe two respective detector cells 5 and 6 are substantially equal and produce an approximative equality of the measured parameters when the gaseous mixture in cell 4 does not include the gas to be measured, so that, in the ray beam emitted from source 1 with a given intensity, the wavelengths corresponding to the absorption band of the gas to be measured pass through said cell 4 without being weakened.
In this case, which corresponds to zero point of the measurement, the absorption in cell 5 of the rays the wave-lengths of, which are those of the middle portions of the lines may be as high as 90%. When subsequently cell 4 is filled with a gaseous mixture which contains some amount of the gas to be measured, this mixture, according to the phenomena above referred to, absorbs chiefly a portion of the rays the wave-lengths of which correspond to the middle portions of the lines. Consequently, the balance which existed before this between the energies absorbed in the two detector cells 5 and 6 no longer exists and there is a higher amount of energy absorbed by cell 6, since the initial balance was based upon the fact that cell 5 received a radiation containing, without any preliminary weakening, therays the wavelengths of which correspond to the middle portions of the lines. The higher the percentage of the gas to be measured in the mixture present in cell 4, the greater the difference between the energies absorbed in cells 5 and 6, so that it is possible accordingly to determine the percentage of gas to be measured in the mixture.
In order to obtain the optimum difference or ratio betweenthese amounts of energies absorbed in cells 5 and 6, for a given concentration of the gas inthe mixture present in cell 4, it is necessary to determine the partial pressure of the receiver gas in said detector cells 5 and- 6, the total pressure in these. cells (when they c'on-tain, in addition to the receiver gas, still another gas which does not absorb the rays that are used to fserve to dilute the first gas and to widen theabsorption lines thereof) and also the height of the cells so that they have predetermined values depending upon the intensity of the radiation and upon the shape of the absorption band of the receiver gas.
Generally, the height of the second detector cell 6 is several times greater than that of the first cell 5.
On the other hand, the height of cell 4 must be determined in such manner that, even for the highest possible concentration of the gas to be measured in the mixture present in this cell, the maximum absorption of the rays the wave-length of which corresponds to the middle portions of the lines or" the absorption band of the gas to be measured does not exceed a predetermined percentage. The value of this percentage may be for instance 20% and this for the more intensive lines which,
for measurements according to the present invention, are
"the only ones to be taken into account.'
By way of indication, I will now give the heights of cells 4, 5 and 6 used for determining the proportion of carbon monoxide (CO) in a mixture of said gas with.
nitrogen (N where the relative amount of CO was about 4%. In this case, cells 5 and 6 were filled with 'ratus. parent bottom and to dispose across the same beam other a mixture of CO and N in which the percentage of CO was 11%. The height of cell 4- was 25 mm., that of cell 5, 10 mm. and that of cell 6, 25 mm. For pressures of the mixture in cells 5 and 6 ranging from 400 mm. to 600 mm. of mercury, the sensitiveness (measurement effect) was practically constant.
It should further be noted that the means according to the invention have the advantage of a high selectivity. As a matter of fact, the absorbed energy due to the presence of a disturbing gas having an absorption band which overlaps that of the gas to be measured is generally more or less the same in the two detector cells and is therefore at least partly compensated for. It should be noted here that the measurement effect obtained with the device according to my invention is due to the preferential absorption bythe first detector cell of rays the wave-lengths of which correspond to the middle portions of the most intensive lines of the absorption band of the gas to be measured, whereas this preferential effect does not act for the parasitic absorption of the disturbing gas if the middle portions of the lines which overlap only by their edges are sufiiciently spaced apart.
In the contrary case, that is to say if compensation were not complete, the invention easily permits of taking supplementary compensatory steps, such for instance as filtering by gaseous layers constituted by disturbing gases and interposed across the path of travel of the beam, either before cell 5 or between cells 5 and 6.
When the residual disturbing effect isinegative, it may be compensated by adding to the receiver gas some amount of the disturbing gas so as to produce a positive compensation efiect of the same magnitude.
The advantages of the device according to my invention are considerable. They permit, with an apparatus much simpler and much less expensive, of obtaining, as to stability and selectivity of-the measurement, better results than with the known methods. 1
They make it possible, due to the higher stability they ensure, to construct easily apparatus having an automatic compensation at zero, by acting through a servo-mechanism on shutter 11. In this case, the desired concentration is indicated by the position of shutter 11.
Furthermore, the fact of using for measurement of a gas in a mixture only the rays the wave-lengths of which are located inside the absorption bands thereof, permits of using the other rays of the same beamfor simultaneously analyzing other components in the same appa- Itthen suflices to provide cell 6 with a transpairs of detector cells filled with other gases. 7
It has been explained above that the amount of energy absorbed from the ray beam in cell 4 must not exceed a given maximum averaging 20% when the apparatus 10 gives the difference between the energies absorbed respectively in cells 5 and 6, as shown by Fig; 1. As a rule, there is no' difliculty in complying with this condition. However, for some analysis problems, a difliculty may occur. 5
For instance, if it is desired to measure traces of a gas in a mixture, the height of the cell 4 containing this mixture must be sufliciently great to give the sensitiveness necessary for measurement of concentrations which are normally very low. However it may happen, in some industrial applications, that, for accidental causes, the concentration of the gas to be measured increases suddenly beyond the limit that has been expected and the measurement may then become ambiguous because the difierence of the absorptions in cells 5 and 6 starts decreasing when the rays are more and more absorbed in the cell which contains the mixture. i
For instance, in an'apparatus such as above described ,-mm., to measure percentages of carbon monoxide not higher than 0.1%,; the; same signal of 10 mv. is obtained in apparatus 10 for values of the percentage of equal respectively to 0.1 and to 10.
In order. to remove ,any possibility of ambiguity of the measureinrllir t then necessaryfto determine, in addition to the difference betweentheener'gies absorbed in' cells 5, and .6, the absolute value of the energy selectively absorbedincell, 6.. Inthiscaseit is particularly advantageous to -.measure r the;ratio, p f the signal correspondingto said difiernceQ-and of the signal correspending "to the energy selectively absorbed in said Fig. 2 shows an apparatus for measuring this ratio. The elements of the apparatus of Fig. 2 which have already been shown on Fig. 1 are designated by the same reference numerals.
In this case, the ray beam which passes through cells 4, and 6 is not only periodically cut off at a given frequency, before entering cell 5, but also once more periodically cut off with a different frequency as it is passing between cells 5 and 6. The first mentioned interruption of the ray beam is obtained, in Fig. 1, by a rotating shutter 2 located upstream of cell 4. In the construction of Fig. 2, the same effect is obtained by a shutter 12 located between cell 4 and cell 5. The second intermption of the beam is obtained by means of another shutter 13 disposed between cells 5 and 6. The two shutters 12 and 13 may be fixed to the same shaft and driven by the same motor 3. However the frequencies of interruption must be different for the two elements 12 and 13.
The first shutter 12 gives a frequency of interruption of the beam leaving cell 4 equal to h, whereas the second shutter 13 gives-a frequency of interruption f; for a portion of the beam entering cell 6.
Fig. 3 shows a construction of shutter 12, the circle in dotted lines indicating the cross section s of the beam. Fig. 4 shows a construction of shutter 13 which acts only upon a portion of the cross section s of the beam and which gives for instance a frequency f =3f Of course, shutter 12, instead of being located between cells 4 and 5, might have been disposed between source 1 and cell 4. V
The amounts of energy due to selective ray absorption in cells 5 and 6 act upon the opposed faces of the movable diaphragm 7 of the diaphragm condenser.
Due to the factthat the beam is interrupted twice with different frequencies, I obtain two signals. The first one, designated by e is a differential signal of frequency f;, and the second one, designated by 2 and superimposed upon the first one, has a frequency 3. The two signals e and e after being amplified in amplifier 9, are separated and rectified through a known device 14- 15 containing filtering means. Their ratio is measured by a potentiometric measurement instrument 16.
By means of an adjustable shutter 11, it is possible to adjust the apparatus so that the differential signal e is zero when the concentration of the gas to be measured in cell 4 is zero. This signal e increases in accordance with the concentration of this gas in said cell 4.
On the contrary, signal e of frequency f remains practically constant for normal variations of the concentration of the gas to be measured and starts decreasing only if this concentration is substantially in excess of the normal concentration value. If the absorption in cell 4 exceeds the limit that has been fixed, the reduction of the rays selectively absorbed in cells 5 and 6 has an analogous effect on the two signals e and e whereby the ratio measured by instrument 16 keeps increasing and does not risk to become ambiguous.
Another method for measuring the ratio of signals e and 2 would consist in producing a single frequency of interruption with the twoshutters 12 and 13 but in bringing these two interruptions in difference of phase, so
that the two'signals e and e; can be separated by phase discrimination by means of synchronized switches. What ever be the. means used for measuring the ratio of the two signals e; and e Ieliminate not only any ambiguityintheresult off the measurement but I obtain at the same time that the 'resultof the measurement is still less influencedby the possible presence'in themixture of other'gases having absorption bands overlapping those of the gas to be, measured. Asa matter of fact, the absorption produced by such gases reduces boththe main signal and the auxiliary signal so that" the ratio remains practically unchanged.
Furthermore, by measuring the ratio of the two signals, the measurement becomes independent of the variations that may be undergone either by the intensity of the source of the ray beam or by the amplification.
Instead of using the signal e by measuring the ratio of signals e, and e I might, in some cases, merely observe the importance of the selective absorption in the second detector cell 6. As a matter of fact, the fact that this absorption undergoes an important reduction indicates that the result of the measurement may become ambiguous. In this case, the measurement of the absorption in cell 6 alone serves to give a warning signal.
In a general manner, while I have, in the above description, disclosed what I deem to be practical and elficient embodiments of my invention, it should be well understood that I do not wish to be limited thereto as there might be changes made in the arrangement, disposit-ion and form of the parts Without departing from the principle of the present invention as comprehended within the scope of the accompanying claims. For instance, the two detector cells are not necessarily both connected with a differential element such as a diaphragm condenser. They might remain separate from each other.
Also, the invention does not exclude the case where the gases present in the detector cells have different pressures and concentrations so as to facilitate measurement.
What I claim is:
l. A fluid analyzer apparatus for measuring the relative amount, in amixture of fluids, of a given fluid component capable of selectively absorbing rays of given wave bands from a given ray beam passing therethrough, which comprises, in combination, a sample cell arranged to be filled with said fluid mixture to be analyzed, two detector cells both containing the same fluid, said last mentioned fluid having substantially the same ray absorption wave bands as said component, means for passing the same ray beam through said sample cell and both of said detector cells in series, and means connected to both said detector cells for comparing the respective amounts of energy absorbed by said two detector cells from said ray beam.
2. An apparatus according to claim 1 in which the dimension of the first detector cell in the direction in which said beam travels therethrough is smaller than the corresponding dimension of the second detector cell.
3. A fluid analyzer apparatus for measuring the relative amount, in a mixture of fluids, of a given fluid component capable of selectively absorbing rays of given wave bands from a given rays beam passing theremeans connected to both said detector cells for measuring the difference between the respective amounts of energy absorbed by said two detector cells from said ray beam.
4. An apparatus according to claim 3 further including a shutter disposed between said two detector cells 7 and adjustable to indicate the concentration of the gas to'be measured when the same amounts of energy are absorbed from -said'two detector cells, respectively. 151 An apparatus according to claim 3' further includ ing. 'means' for measitring the. absoluterv alue of the amount of energy. absorbed from said' ray beam by the lastjdeteetorcelhv. a I 1 a 16 An apparatl is according to claim 5 'in which the two last mentioned means are means for producing signals re'stiec't-ively proportional to the difference, of the amounts of energy absorbed from-said two detector .cell
8 and to the amount of energy, absorbed by the last men.- t ioned'cell. I I lieierehcesi-Ci tedin the 'file of this patent I j' a NI ED S A PAT NT
US582875A 1955-05-07 1956-05-04 Devices for analyzing fluid mixtures by absorption of rays Expired - Lifetime US2951939A (en)

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US3084253A (en) * 1960-09-06 1963-04-02 Barnes Eng Co Continuously self-calibrating differential detection system
US3121790A (en) * 1959-10-09 1964-02-18 Distillers Co Yeast Ltd Infrared analyser with signal ratio indicating means
US3161768A (en) * 1961-01-27 1964-12-15 Nat Res Dev Method and apparatus for the analysis of emulsions and suspensions
US3162761A (en) * 1960-06-03 1964-12-22 Onera (Off Nat Aerospatiale) Apparatus for analyzing a mixture of substances by selective absorption of infrared radiation
US3171027A (en) * 1961-06-26 1965-02-23 Wallack Stanley Infrared atmospheric contamination detector system with the detector interrupted at a sub-harmonic frequency of the source
US3193676A (en) * 1961-12-15 1965-07-06 Parsons & Co Sir Howard G Infra-red gas analysers
US3245261A (en) * 1961-11-07 1966-04-12 Ici Ltd Temperature measurement of plastic film
US3476934A (en) * 1966-07-27 1969-11-04 Onera (Off Nat Aerospatiale) Infra-red gas analyzer for measuring the concentration of a particular gas
US3740555A (en) * 1968-07-22 1973-06-19 Hartmann & Braun Ag Twin beam infrared absorption analyzer
US4306153A (en) * 1979-03-15 1981-12-15 Hartmann & Braun Aktiengesellschaft Nondispersive infrared gas analyzer
US4742229A (en) * 1985-06-28 1988-05-03 Siemens Aktiengesellschaft Pneumatic detector for nondispersive infrared gas analyzers
US4817013A (en) * 1986-10-17 1989-03-28 Nellcor, Inc. Multichannel gas analyzer and method of use
US5559333A (en) * 1993-11-29 1996-09-24 Shimadzu Corporation Apparatus of non-dispersive infrared analyzer

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE9014162U1 (en) * 1990-10-11 1990-12-20 Siemens Ag, 8000 Muenchen, De
DE19608907C1 (en) * 1996-03-07 1997-04-03 Siemens Ag Non-dispersive gas analyser

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GB698023A (en) * 1900-01-01
GB645576A (en) * 1948-10-06 1950-11-01 Parsons C A & Co Ltd Improvements in or relating to infra-red gas analysing apparatus
US2674696A (en) * 1952-11-12 1954-04-06 Shell Dev Infrared gas analyzer
US2688089A (en) * 1952-06-17 1954-08-31 Perkin Elmer Corp Radiation instrument

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Publication number Priority date Publication date Assignee Title
GB698023A (en) * 1900-01-01
GB645576A (en) * 1948-10-06 1950-11-01 Parsons C A & Co Ltd Improvements in or relating to infra-red gas analysing apparatus
US2688089A (en) * 1952-06-17 1954-08-31 Perkin Elmer Corp Radiation instrument
US2674696A (en) * 1952-11-12 1954-04-06 Shell Dev Infrared gas analyzer

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3121790A (en) * 1959-10-09 1964-02-18 Distillers Co Yeast Ltd Infrared analyser with signal ratio indicating means
US3162761A (en) * 1960-06-03 1964-12-22 Onera (Off Nat Aerospatiale) Apparatus for analyzing a mixture of substances by selective absorption of infrared radiation
US3084253A (en) * 1960-09-06 1963-04-02 Barnes Eng Co Continuously self-calibrating differential detection system
US3161768A (en) * 1961-01-27 1964-12-15 Nat Res Dev Method and apparatus for the analysis of emulsions and suspensions
US3171027A (en) * 1961-06-26 1965-02-23 Wallack Stanley Infrared atmospheric contamination detector system with the detector interrupted at a sub-harmonic frequency of the source
US3245261A (en) * 1961-11-07 1966-04-12 Ici Ltd Temperature measurement of plastic film
US3193676A (en) * 1961-12-15 1965-07-06 Parsons & Co Sir Howard G Infra-red gas analysers
US3476934A (en) * 1966-07-27 1969-11-04 Onera (Off Nat Aerospatiale) Infra-red gas analyzer for measuring the concentration of a particular gas
US3740555A (en) * 1968-07-22 1973-06-19 Hartmann & Braun Ag Twin beam infrared absorption analyzer
US4306153A (en) * 1979-03-15 1981-12-15 Hartmann & Braun Aktiengesellschaft Nondispersive infrared gas analyzer
US4742229A (en) * 1985-06-28 1988-05-03 Siemens Aktiengesellschaft Pneumatic detector for nondispersive infrared gas analyzers
US4817013A (en) * 1986-10-17 1989-03-28 Nellcor, Inc. Multichannel gas analyzer and method of use
US5559333A (en) * 1993-11-29 1996-09-24 Shimadzu Corporation Apparatus of non-dispersive infrared analyzer

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GB849831A (en) 1960-09-28
FR69345E (en) 1958-10-23
FR1132413A (en) 1957-03-11

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